18 month update

[Guest guest]

Hi All,

This is my 18 month update. Just to give a little history, I am a

32 year old male who was diagnosed with Relapsing-Remitting MS in

October of 2001. I was on the CRABS for three years. I quickly

deteriorated in particular toward the end of that time, winding up

in a wheelchair and for 5 months and legally blind for 18 months.

Three months into my wheel chair nightmare, I was surfing the

internet and stumbled across information on a drug called LDN. Two

months later I stopped taking the CRABS completely and began started

the LDN. In less than a week, I was out of the wheelchair yet still

using the walls to walk and balance myself. Being determined, I

began to exercise at home, I was able to stand-up showers, started

the Swank diet, and continued a strict vitamin regimen.

Now after 18 months on LDN, I mow my own grass with a self-

propelled mower, my vision impairment has improved enough that I

have just been approved to drive during daylight hours. I also

attend aqua therapy at the YMCA three times a week while exercising

at home another three days during the week. I live alone and

perform my own housework. I anticipate that in mid-summer I will

start physical therapy. Overall, I do very well managing the

symptoms with the LDN. My worst day now is much better than my best

day pre-LDN.

During this entire time since my diagnosis, I have maintained the

attitude that I would rather try and fail 1,000 times than never try

at all. I am so thankful that I got off the CRABS and started LDN.

To any and all people that are still on the fence or researching LDN

use for their condition, I urge you to go ahead and start it now

while continuing your research. It has already been shown that LDN

is not harmful however, most individuals on this forum who have

already started using LDN regret that they did not start it sooner.

C

" …My future's so bright I've got to wear shades… "